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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

AE1102 — IVDD — General IVDD by OÜ InterVacTechnology

MD Atlas
OÜ InterVacTechnology

EUDAMED last updated this device on Feb 19, 2026

AE1102

B-04744489015594

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: OÜ InterVacTechnology
UDI-DI code: 04744489015594
Reference / catalog number: AE1102

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Manufacturer information

Organization name: OÜ InterVacTechnology
SRN: EE-MF-000001021
Manufacturer status: Active

Market distribution

Primary placement in Estonia; available across 1 country total.

Placed on the market in Estonia; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04744489015594
Basic UDI-DI: B-04744489015594
Reference / catalog number: AE1102
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Vacuum blood collection tube Lind-Vac® 13x75 mm, Clot Activator, 1 ml, red cap, sterile, two-part
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W050101010201BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

AE1202B-04744489012562On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.